首页> 外文期刊>Archives of dermatological research. >Major translocation of calcium upon epidermal barrier insult: imaging and quantification via FLIM/Fourier vector analysis.
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Major translocation of calcium upon epidermal barrier insult: imaging and quantification via FLIM/Fourier vector analysis.

机译:钙在表皮屏障损伤后的主要移位:通过FLIM / Fourier载体分析进行成像和定量。

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Calcium controls an array of key events in keratinocytes and epidermis: localized changes in Ca(2+) concentrations and their regulation are therefore especially important to assess when observing epidermal barrier homeostasis and repair, neonatal barrier establishment, in differentiation, signaling, cell adhesion, and in various pathological states. Yet, tissue- and cellular Ca(2+) concentrations in physiologic and diseased states are only partially known, and difficult to measure. Prior observations on the Ca(2+) distribution in skin were based on Ca(2+) precipitation followed by electron microscopy, or proton-induced X-ray emission. Neither cellular and/or subcellular localization could be determined through these approaches. In cells in vitro, fluorescent dyes have been used extensively for ratiometric measurements of static and dynamic Ca(2+) concentrations, also assessing organelle Ca(2+) concentrations. For lack of better methods, these findings together build the basis for the current view of the role of Ca(2+) in epidermis, their limitations notwithstanding. Here we report a method using Calcium Green 5N as the calcium sensor and the phasor-plot approach to separate raw lifetime components. Thus, fluorescence lifetime imaging (FLIM) enables us to quantitatively assess and visualize dynamic changes of Ca(2+) at light-microscopic resolution in ex vivo biopsies of unfixed epidermis, in close to in vivo conditions. Comparing undisturbed epidermis with epidermis following a barrier insult revealed major shifts, and more importantly, a mobilization of high amounts of Ca(2+) shortly following barrier disruption, from intracellular stores. These results partially contradict the conventional view, where barrier insults abrogate a Ca(2+) gradient towards the stratum granulosum. Ca(2+) FLIM overcomes prior limitations in the observation of epidermal Ca(2+) dynamics, and will allow further insights into basic epidermal physiology.
机译:钙控制角质形成细胞和表皮中的一系列关键事件:Ca(2+)浓度的局部变化及其调节因此对评估观察表皮屏障的稳态和修复,新生儿屏障的建立,分化,信号传导,细胞粘附,并处于各种病理状态。但是,在生理和疾病状态下组织和细胞中Ca(2+)的浓度仅是部分已知的,很难测量。关于Ca(2+)在皮肤中的分布的先前观察是基于Ca(2+)沉淀,然后是电子显微镜或质子诱导的X射线发射。通过这些方法都不能确定细胞和/或亚细胞的定位。在体外细胞中,荧光染料已广泛用于静态和动态Ca(2+)浓度的比例测量,还可以评估细胞器Ca(2+)的浓度。由于缺乏更好的方法,这些发现共同为当前表皮中Ca(2+)的作用奠定了基础,尽管存在局限性。在这里,我们报告了一种使用Calcium Green 5N作为钙传感器和相量图方法来分离原始寿命成分的方法。因此,荧光寿命成像(FLIM)使我们能够定量地评估和可视化Ca(2+)的动态变化,在接近活体条件的情况下,在未固定表皮的活检中以光学显微镜的分辨率观察。比较不受干扰的表皮与屏障侵害后的表皮揭示了主要变化,更重要的是,屏障破坏后不久,从细胞内存储动员了大量的Ca(2+)。这些结果在一定程度上与常规观点相矛盾,在常规观点中,屏障侮辱消除了朝向颗粒层的Ca(2+)梯度。 Ca(2+)FLIM克服了表皮Ca(2+)动力学观察中的先前限制,并将允许进一​​步洞察基本的表皮生理。

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